ClearanceBrief
510(k) K052581 ยท KGI Densitometer, Bone

LUNAR IDXA

ApplicantGe Medical Systems Ultrasound and Primary Care Dia, Madison WI, US
DecisionSubstantially Equivalent, Oct 20, 2005
ReceivedSep 20, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052581

DateFirm and productCodeLinked 510(k)
Apr 24, 2020GE Healthcare, LLC
Lunar iDXA bone densitometer
Open, Classified
KGINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.